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Polymer-Based DNA Delivery Systems for Cancer Immunotherapy

The use of gene delivery systems for the expression of antigenic proteins is an established means for activating a patient’s own immune system against the cancer they carry. Since tumor cells are poor antigen-presenting cells, cross-presentation of tumor antigens by dendritic cells (DCs) is essentia...

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Detalles Bibliográficos
Autores principales: David, Ayelet, Golani-Armon, Adi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153417/
http://dx.doi.org/10.1007/978-1-4939-3634-2_10
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author David, Ayelet
Golani-Armon, Adi
author_facet David, Ayelet
Golani-Armon, Adi
author_sort David, Ayelet
collection PubMed
description The use of gene delivery systems for the expression of antigenic proteins is an established means for activating a patient’s own immune system against the cancer they carry. Since tumor cells are poor antigen-presenting cells, cross-presentation of tumor antigens by dendritic cells (DCs) is essential for the generation of tumor-specific cytotoxic T-lymphocyte responses. A number of polymer-based nanomedicines have been developed to deliver genes into DCs, primarily by incorporating tumor-specific, antigen-encoding plasmid DNA with polycationic molecules to facilitate DNA loading and intracellular trafficking. Direct in vivo targeting of plasmid DNA to DC surface receptors can induce high transfection efficiency and long-term gene expression, essential for antigen loading onto major histocompatibility complex molecules and stimulation of T-cell responses. This chapter summarizes the physicochemical properties and biological information on polymer-based non-viral vectors used for targeting DCs, and discusses the main challenges for successful in vivo gene transfer into DCs.
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spelling pubmed-71534172020-04-13 Polymer-Based DNA Delivery Systems for Cancer Immunotherapy David, Ayelet Golani-Armon, Adi Nanomedicine Article The use of gene delivery systems for the expression of antigenic proteins is an established means for activating a patient’s own immune system against the cancer they carry. Since tumor cells are poor antigen-presenting cells, cross-presentation of tumor antigens by dendritic cells (DCs) is essential for the generation of tumor-specific cytotoxic T-lymphocyte responses. A number of polymer-based nanomedicines have been developed to deliver genes into DCs, primarily by incorporating tumor-specific, antigen-encoding plasmid DNA with polycationic molecules to facilitate DNA loading and intracellular trafficking. Direct in vivo targeting of plasmid DNA to DC surface receptors can induce high transfection efficiency and long-term gene expression, essential for antigen loading onto major histocompatibility complex molecules and stimulation of T-cell responses. This chapter summarizes the physicochemical properties and biological information on polymer-based non-viral vectors used for targeting DCs, and discusses the main challenges for successful in vivo gene transfer into DCs. 2016-05-28 /pmc/articles/PMC7153417/ http://dx.doi.org/10.1007/978-1-4939-3634-2_10 Text en © Controlled Release Society 2016 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
David, Ayelet
Golani-Armon, Adi
Polymer-Based DNA Delivery Systems for Cancer Immunotherapy
title Polymer-Based DNA Delivery Systems for Cancer Immunotherapy
title_full Polymer-Based DNA Delivery Systems for Cancer Immunotherapy
title_fullStr Polymer-Based DNA Delivery Systems for Cancer Immunotherapy
title_full_unstemmed Polymer-Based DNA Delivery Systems for Cancer Immunotherapy
title_short Polymer-Based DNA Delivery Systems for Cancer Immunotherapy
title_sort polymer-based dna delivery systems for cancer immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153417/
http://dx.doi.org/10.1007/978-1-4939-3634-2_10
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